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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 966529Generated: October 30, 2026

Diisobutylamine → 5-(2-Diisobutylamino-ethyl)-2-methyl-1H-indole-3-carboxylic Acid Benzyl Ester

https://huagongshe.com/reaction/966529

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisobutylamineHCID 8085—
Reactant5-(2-Methanesulfonyloxy-ethyl)-2-methyl-1H-indole-3-carboxylic Acid Benzyl EsterHCID 23393852—
Solvent1,4-DioxaneHCID 31275—
Product5-(2-Diisobutylamino-ethyl)-2-methyl-1H-indole-3-carboxylic Acid Benzyl EsterHCID 1020233377.5%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 5-(2-methanesulfonyloxy-ethyl)-2-methyl-1H-indole-3-carboxylic acid benzyl ester (360 mg, 0.93 mmol, Example 56, Step D) in dioxane (10 mL) was added diisobutylamine (1.62 mL, 9.3 mmol). The mixture was stirred at 100° C. overnight and then partitioned between methylene chloride and water. The organic phase was washed with water and brine, dried over Na2SO4 and filtered. The filtrate was concentrated in vacuo to give a solid residue, which was purified by chromatography (20% ethyl acetate in hexanes) to give 303 mg (77%) of the desired product as a white solid: mp 134-135° C.; MS(APCI+): m/z 421.3 (MH+); Anal. Calcd for C27H36N2O2: C, 77.10; H, 8.63; N, 6.66. Found: C, 76.94; H, 8.75; N, 6.55.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06951848B2
Source datasetuspto-grants-2005_10
ORD IDord-d2c47aef91744d27b9933cd9d7213eb3
Source noteuspto-grants-2005_10